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E Seidman

Showing results (521-530 of 533) with videos related to

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NPJ Genomic Medicine|August 23, 2018
An integrated clinical program and crowdsourcing strategy for genomic sequencing and Mendelian disease gene discoveryAlireza Haghighi, Joel B Krier, Agnes Toth-Petroczy, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 17, 2012
A public resource facilitating clinical use of genomesMadeleine P Ball, Joseph V Thakuria, Alexander Wait Zaranek, et al.
Circulation. Genomic and Precision Medicine|August 21, 2020
Genetic Studies of Hypertrophic Cardiomyopathy in Singaporeans Identify Variants in <i>TNNI3</i> and <i>TNNT2</i> That Are Common in Chinese PatientsChee Jian Pua, Nevin Tham, Calvin W L Chin, et al.
Nature|May 14, 2013
De novo mutations in histone-modifying genes in congenital heart diseaseSamir Zaidi, Murim Choi, Hiroko Wakimoto, et al.
Science (New York, N.Y.)|August 4, 2022
Pathogenic variants damage cell composition and single cell transcription in cardiomyopathiesDaniel Reichart, Eric L Lindberg, Henrike Maatz, et al.
Circulation|April 17, 2019
Genetic Variants Associated With Cancer Therapy-Induced CardiomyopathyPablo Garcia-Pavia, Yuri Kim, Maria Alejandra Restrepo-Cordoba, et al.
Cell|June 4, 2019
The Translational Landscape of the Human HeartSebastiaan van Heesch, Franziska Witte, Valentin Schneider-Lunitz, et al.
Nature|November 22, 2017
IL-11 is a crucial determinant of cardiovascular fibrosisSebastian Schafer, Sivakumar Viswanathan, Anissa A Widjaja, et al.
Cell|January 13, 2023
Loss of epigenetic information as a cause of mammalian agingJae-Hyun Yang, Motoshi Hayano, Patrick T Griffin, et al.
European Heart Journal|March 7, 2021
Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23Sophie Garnier, Magdalena Harakalova, Stefan Weiss, et al.
Pageof 54

Showing results (521-530 of 533) with videos related to

Sort By:
Pageof 54
NPJ Genomic Medicine|August 23, 2018
An integrated clinical program and crowdsourcing strategy for genomic sequencing and Mendelian disease gene discoveryAlireza Haghighi, Joel B Krier, Agnes Toth-Petroczy, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 17, 2012
A public resource facilitating clinical use of genomesMadeleine P Ball, Joseph V Thakuria, Alexander Wait Zaranek, et al.
Circulation. Genomic and Precision Medicine|August 21, 2020
Genetic Studies of Hypertrophic Cardiomyopathy in Singaporeans Identify Variants in <i>TNNI3</i> and <i>TNNT2</i> That Are Common in Chinese PatientsChee Jian Pua, Nevin Tham, Calvin W L Chin, et al.
Nature|May 14, 2013
De novo mutations in histone-modifying genes in congenital heart diseaseSamir Zaidi, Murim Choi, Hiroko Wakimoto, et al.
Science (New York, N.Y.)|August 4, 2022
Pathogenic variants damage cell composition and single cell transcription in cardiomyopathiesDaniel Reichart, Eric L Lindberg, Henrike Maatz, et al.
Circulation|April 17, 2019
Genetic Variants Associated With Cancer Therapy-Induced CardiomyopathyPablo Garcia-Pavia, Yuri Kim, Maria Alejandra Restrepo-Cordoba, et al.
Cell|June 4, 2019
The Translational Landscape of the Human HeartSebastiaan van Heesch, Franziska Witte, Valentin Schneider-Lunitz, et al.
Nature|November 22, 2017
IL-11 is a crucial determinant of cardiovascular fibrosisSebastian Schafer, Sivakumar Viswanathan, Anissa A Widjaja, et al.
Cell|January 13, 2023
Loss of epigenetic information as a cause of mammalian agingJae-Hyun Yang, Motoshi Hayano, Patrick T Griffin, et al.
European Heart Journal|March 7, 2021
Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23Sophie Garnier, Magdalena Harakalova, Stefan Weiss, et al.
Pageof 54